A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518068



Internal ID294464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6689302..6689362hg38UCSC Ensembl
chr19:6689313..6689373hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720956
Samples
Known GenesC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518068
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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